A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278026



Internal ID20845066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42120097..42124293hg38UCSC Ensembl
chr8:41977615..41981811hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg384197
hg194197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278026
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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